You are here

Home » Content

OSTEOGENEZİS İMPERFEKTA: BİR OLGU SUNUMU

OSTEOGENESIS IMPERFECTA: A CASE REPORT

Journal Name:

  • Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi

Publication Year:

  • 2007

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Osteogenesis imperfecta, or brittle bone disease, is a heritable disorder characterized by increased bone fraglitty. This article reports the case of a 7 year old child diagnosed with type I osteogenesis imperfecta, assessing the cinnical features observed, with emphasis on the histological, oral and dental findings. The histological examination of dentin often reveals presence of irregular dentinal tubules, amorphous areas and poor calcification. All caries teeth treated with stainless steel crowns. The extreme bone fraglitty seen in patients suffering from osteogenesis imperfecta pose a series of problems with regard to behavior management and rendernng of quaitty dental treatment.
Bookmark/Search this post with
Abstract (Original Language): 
Osteogenezis imperfekta veya krrigan kemik hastalığı, kemik kağanlığında artış ile karakterize kalttımsal brr bozukluktur. Bu olgu raporunda tip I tansı konan 7 yaşında brr çocuğun diş, ağız ve histolojik bulguları vurgulanmıştır ve kiinik özelikkleri değerlendirilmiştir. Dentinin histolojik incelenmesinde, zayıfkalsifiye olmuş, şekilsiz aaanaar ve düzensiz dentin tubulleri gözlemlenmiştir. Çürük dişler, paslanmaz çeiik kuronlar kullanılarak restore edilmiştir. Bu hastalar, şiddetli kemik kırı/ma/arından zarar gördüklerinden dolayı, nitelikli diş tedavilerini sağlamak ve davranış yönetimi hususunda bir dizi sorunlar üzerinde durmak gereklidir.
FULL TEXT (PDF): 
PDF icon arastirmax-osteogenezis-imperfekta-bir-olgu-sunumu.pdf
  • 3
48-51
  • Turkish

REFERENCES

References: 

1.
Akal N, Değer Ö. Oligodonti ile Birlikte Görülen Osteogenezis Imperfecta. G.ÜÜ. Dişhekimliği Faküttesi Dergisi 1992; 9:149-161.
2. Gage JP, Francis MJO, Smith R. Abnormal amino acid analyses obtained from osteogenesis imperfecta dentnn. J Dent Res 1988; 67: 1097¬1102.
3. Gupte T, Iyer V, Dam/e SG, Maikk N, Ha/be A. Osteogenesis imperfecta. J Indian Soc Pedod Prev Dent. 2006; 24: S44-46.
4. Huber MA. Osteogenesis imperfecta. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007; 103:314-320.
5. Kindelan J, Tobnn M, Roberts-Harry D, Loukota RA. Orthodontic and orthognathic management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta: a case report. J Orthod2003; 30:291-296.
6. Koreeda-Mnnra M,Oaishi T, Oshima T. Significance of histopathologic examination in the diagnosis of dentin defects associated with type IV osteogenesis imperfecta. Two case reports.
GÜRBÜZ, ÖZBEK, ÖZBEK
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003; 95:85-89.
7. Malmgren B, Norgren S. Dental aberrations in children and adolescents with osteogenesis imperfecta. Acta Odontol Scand2002; 60: 65-71.
8. Malmgren B, Lindskog S. Assessment of dysplastc dentin in osteogenesis imperfecta and dentinogenesis imperfecta. Acta Odontol Scand 2003; 61:72-80.
9. Marini JC. Osteogenesis imperfecta: comprehensive management. Adv Pediatr 1988; 35: 391-426.
10.
Öztunç H, Üstün Y. Osteogenezis Imperfekta: Brr Olgu Raporu. Cumhuriyet Üniversitesi Dişhekimliği Faküttesi Dergisi2000; 3:133-135.
11. Petersen K, Wetzel WE. Recent findings in classification of osteogenesis imperfecta by means of existing dental symptoms. J Dent Child 1998; 65:305-359.
12. Primorac D, Rowe DW, Mottes M, Barisic I, Anticevic D, Mrrandola S, Gomez Lrra M, KaaajzicI, Kusec V, Glorieux FH. Osteogenesis imperfecta at the beginning of bone and joint decade. Croat Med J 2001; 42:393-415.
13. Sanches K, de Queiroz AM, de Frettas AC, Serrano KV. Ciinical features, dental findings and dental care management nn osteogenesis imperfecta. J Cin Pediatr Dent2005; 30: 77-82.
14. Sodeman Jr WA, Sodeman TM. Sodeman's Pathologic Physiology. 7th ed, Philadelphia: WB Saunders, 1985: 717.
15. Ward LM, Rauch F, Travers R, Chabot G, Azouz EM, Laic L, Rougheey PJ, Glorieux FH. Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease. Bone 2002; 31:12-18.

Thank you for copying data from http://www.arastirmax.com